Zobrazeno 1 - 10
of 417
pro vyhledávání: '"Robert C, Griggs"'
Autor:
Robert C. Griggs, M. Maral Mouradian
Publikováno v:
Neurotherapeutics, Vol 21, Iss 4, Pp e00385- (2024)
Externí odkaz:
https://doaj.org/article/5a0101ea07cf453ca53bc231af2bcedc
Association between neurodevelopmental impairments and motor function in Duchenne muscular dystrophy
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 12, Pp 2285-2296 (2023)
Abstract Objective We explored various prognostic factors of motor outcomes in corticosteroid‐naive boys with Duchenne Muscular Dystrophy (DMD). Methods The associations between parent‐reported neurodevelopmental concerns (speech delay, speech an
Externí odkaz:
https://doaj.org/article/79829bd13c7b40b88426668627dcff0f
Autor:
Lauren B. Reoma, Ania Busza, M. Maral Mouradian, Petra Kaufmann, Erika F. Augustine, Samuel Frank, Thomas P. Sutula, Andrew J. Cole, Heather D. Fitter, William Meurer, Avindra Nath, Robert C. Griggs
Publikováno v:
Annals of Neurology. 93:427-430
The subspecialty of Experimental Neurotherapeutics trains neurologists in discovering and developing new treatments for neurologic diseases. Based on development of exciting new treatments for genetic and inflammatory diseases, we predict that there
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77cab21cac220cc1c23dd3e8575a5686
https://doi.org/10.1002/ana.26582
https://doi.org/10.1002/ana.26582
Autor:
Rebecca A. Crow, Kimberly A. Hart, Michael P. McDermott, Rabi Tawil, William B. Martens, Barbara E. Herr, Elaine McColl, Jennifer Wilkinson, Janbernd Kirschner, Wendy M. King, Michele Eagle, Mary W. Brown, Deborah Hirtz, Hanns Lochmuller, Volker Straub, Emma Ciafaloni, Perry B. Shieh, Stefan Spinty, Anne-Marie Childs, Adnan Y. Manzur, Lucia Morandi, Russell J. Butterfield, Iain Horrocks, Helen Roper, Kevin M. Flanigan, Nancy L. Kuntz, Jean K. Mah, Leslie Morrison, Basil T. Darras, Maja von der Hagen, Ulrike Schara, Ekkehard Wilichowski, Tiziana Mongini, Craig M. McDonald, Giuseppe Vita, Richard J. Barohn, Richard S. Finkel, Matthew Wicklund, Hugh J. McMillan, Imelda Hughes, Elena Pegoraro, W. Bryan Burnette, James F. Howard, Mathula Thangarajh, Craig Campbell, Robert C. Griggs, Kate Bushby, Michela Guglieri
Publikováno v:
Trials, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Background Trials in rare diseases have many challenges, among which are the need to set up multiple sites in different countries to achieve recruitment targets and the divergent landscape of clinical trial regulations in those countries. Ov
Externí odkaz:
https://doaj.org/article/59fc2ba5f36543fab1efe37a189c7b3f
Publikováno v:
CONTINUUM: Lifelong Learning in Neurology. 28:1817-1834
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::823374426bbc348af481481f44ed06b5
https://doi.org/10.1212/con.0000000000001240
https://doi.org/10.1212/con.0000000000001240
Autor:
Qing, Ke, Youcheng, Zhao, Yuezhou, Li, Jia, Ye, Siyang, Tang, Fangping, He, Fang, Ji, Xuejiao, Dai, Jie, Ni, Yi, Li, Robert C, Griggs, Xiaoyang, Cheng
Publikováno v:
Neuromuscular Disorders. 32:811-819
The non-dystrophic myotonias are inherited skeletal muscle disorders characterized by skeletal muscle stiffness after voluntary contraction, without muscle atrophy. Based on their clinical features, non-dystrophic myotonias are classified into myoton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25a5ff03b1879d40cf4eeaa6a732bd73
https://doi.org/10.1016/j.nmd.2022.08.004
https://doi.org/10.1016/j.nmd.2022.08.004
Autor:
Rabi Tawil, Elaine McColl, Henriette VanRuiten, Anna Mayhew, Marianela Schiava, Rachel Amos, Stephanie Gregory, Tracey Willis, Robert C. Griggs, Michael P. McDermott, Michela Guglieri, Kate Bushby, W. Martens
Publikováno v:
Neurology
Background and ObjectivesDuchenne muscular dystrophy (DMD) is a pediatric neuromuscular disorder caused by mutations in the dystrophin gene. Genotype-phenotype associations have been examined in glucocorticoid-treated boys, but there are few data on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::321a6fdc725debba639a293f3c1c0de6
https://doi.org/10.1212/wnl.0000000000013122
https://doi.org/10.1212/wnl.0000000000013122
Autor:
Valeria A. Sansone, Jeffrey Statland, Nicholas E. Johnson, Michael G. Hanna, Emma Ciafaloni, Fredric Cohen, Perry B Shieh, Robert C. Griggs
Publikováno v:
Muscle & Nerve. 64:342-346
INTRODUCTION/AIM Long-term efficacy and safety of dichlorphenamide (DCP) were characterized in patients with primary periodic paralysis (PPP). METHODS Patients with PPP in a double-blind, placebo-controlled study were randomly assigned to receive DCP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fa010f2a4628a0d1c664cee4191269b
https://doi.org/10.1002/mus.27354
https://doi.org/10.1002/mus.27354
Autor:
Bhaskar Roy, Robert C. Griggs
Publikováno v:
Neurologic Clinics. 39:87-112
Increased understanding of disease pathophysiology and advances in gene therapies and drug technologies are revolutionizing treatment of muscular dystrophies and motor neuron disorders (MNDs). New drugs have been approved for Duchenne muscular dystro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6de4c3f3a4f5ba3255f421c554050a9f
https://doi.org/10.1016/j.ncl.2020.09.005
https://doi.org/10.1016/j.ncl.2020.09.005
Autor:
Sanjeev Rajakulendran, Martin Tristani-Firouzi, Reza Sadjadi, James Cleland, Rabi Tawil, Giovanni Meola, Valeria Sansone, Jaya Trivedi, Stephen C Cannon, Michael G Hanna, Robert C. Griggs
ObjectiveA multi-center, prospective, cross-sectional natural history study to define the clinical phenotype of Andersen-Tawil syndrome, validate its current diagnostic criteria, explore genotype-phenotype correlations, and establish clinically relev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7073c5ed37dd02954a395d003c0e31d2
https://doi.org/10.1101/2022.05.26.22275429
https://doi.org/10.1101/2022.05.26.22275429
